A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637117



Internal ID21829164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22809873..22819308hg38UCSC Ensembl
chr18:20389836..20399271hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg389436
hg199436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637117
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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